orphenadrine citrate
Generic: orphenadrine citrate
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
orphenadrine citrate
Generic Name
orphenadrine citrate
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
orphenadrine citrate 30 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-651
Product ID
25021-651_393d82d5-94f5-43fd-b5c8-d0554795233f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090585
Listing Expiration
2026-12-31
Marketing Start
2011-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021651
Hyphenated Format
25021-651
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
orphenadrine citrate (source: ndc)
Generic Name
orphenadrine citrate (source: ndc)
Application Number
ANDA090585 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/mL
Packaging
- 10 VIAL in 1 CARTON (25021-651-02) / 2 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "393d82d5-94f5-43fd-b5c8-d0554795233f", "openfda": {"unii": ["X0A40N8I4S"], "rxcui": ["994541"], "spl_set_id": ["c8d8596a-b81f-4b83-a2f3-a55922ca4a82"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-651-02) / 2 mL in 1 VIAL", "package_ndc": "25021-651-02", "marketing_start_date": "20111001"}], "brand_name": "Orphenadrine Citrate", "product_id": "25021-651_393d82d5-94f5-43fd-b5c8-d0554795233f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "25021-651", "generic_name": "orphenadrine citrate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Orphenadrine Citrate", "active_ingredients": [{"name": "ORPHENADRINE CITRATE", "strength": "30 mg/mL"}], "application_number": "ANDA090585", "marketing_category": "ANDA", "marketing_start_date": "20111001", "listing_expiration_date": "20261231"}